Viewing Study NCT04666428



Ignite Creation Date: 2024-05-06 @ 3:32 PM
Last Modification Date: 2024-10-26 @ 1:51 PM
Study NCT ID: NCT04666428
Status: COMPLETED
Last Update Posted: 2023-11-29
First Post: 2020-03-16

Brief Title: Effects of Human Papillomavirus Diagnosis on Relationships of Patients With Head and Neck Cancer
Sponsor: Thomas Jefferson University
Organization: Thomas Jefferson University

Study Overview

Official Title: An Observational Study to Determine the Effects of Human Papillomavirus Diagnosis on Relationships of Head and Neck Cancer Patients
Status: COMPLETED
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This trial studies the effects of human papillomavirus diagnosis on the relationships of patients with head and neck cancer Determining the effects of human papillomavirus diagnosis on relationships may determine whether human papillomavirus-positive patients and their partners are more likely to experience decline in relationship intimacy after diagnosis than human papillomavirus-negative patients and their partners This may help researchers provide valuable insight into the degree to which a diagnosis of human papillomavirus affects patient relationships over and above the effects of a cancer diagnosis and address the need for additional patient counseling or education following diagnosis
Detailed Description: PRIMARY OBJECTIVES

I To explore the agreement between patients perceived intimacy level and their partners perceived intimacy level at different time points in the course of their head and neck cancer HNC treatment

II To compare any changes in the patients perceived intimacy scores between human papillomavirus HPV-positive and HPV-negative HNC patients at different time points in the course of their HNC treatment

EXPLORATORY OBJECTIVE

I Identify areas of concern or misinformation among patients and partners where further patient counseling or education may be indicated

OUTLINE

Patients and partners complete surveys over 10 minutes prior to surgery and 3-6 months after completion of treatment

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None